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HumaTurb C+A - FDA Registration ebb61f5df593b2d21d9fa0184ff1f848

Access comprehensive regulatory information for HumaTurb C+A in the Myanmar medical device market through Pure Global AI's free database. This medical device is registered under FDA ID ebb61f5df593b2d21d9fa0184ff1f848 and manufactured by Gesellschaft fรผr Biochemica und Diagnostica mbH. The device was registered on April 07, 2022.

This page provides complete registration details including manufacturer information, authorized representative details, and regulatory compliance data from the official Myanmar FDA medical device database. Pure Global AI offers free access to Myanmar's complete medical device registry.

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FDA Official Data
ebb61f5df593b2d21d9fa0184ff1f848
HumaTurb C+A
FDA ID: ebb61f5df593b2d21d9fa0184ff1f848
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Device Classification
Brand Name
Human
Registration Information
Analysis ID
ebb61f5df593b2d21d9fa0184ff1f848
Registration Date
April 07, 2022